A large collection of various protein phosphatases. Very highly expanded in kinetoplastids.
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 3 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: Q4QHX7
Term | Name | Level | Count |
---|---|---|---|
GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 16 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 16 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 16 |
GO:0016787 | hydrolase activity | 2 | 16 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 16 |
GO:0016791 | phosphatase activity | 5 | 16 |
GO:0017018 | myosin phosphatase activity | 5 | 16 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 16 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 141 | 145 | PF00656 | 0.593 |
CLV_C14_Caspase3-7 | 190 | 194 | PF00656 | 0.705 |
CLV_C14_Caspase3-7 | 588 | 592 | PF00656 | 0.356 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.699 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.326 |
DOC_CYCLIN_RxL_1 | 10 | 23 | PF00134 | 0.491 |
DOC_CYCLIN_yClb3_PxF_3 | 104 | 110 | PF00134 | 0.471 |
DOC_PP1_RVXF_1 | 259 | 266 | PF00149 | 0.645 |
DOC_PP2B_LxvP_1 | 125 | 128 | PF13499 | 0.559 |
DOC_PP4_FxxP_1 | 516 | 519 | PF00568 | 0.300 |
DOC_SPAK_OSR1_1 | 165 | 169 | PF12202 | 0.632 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.706 |
DOC_USP7_MATH_2 | 541 | 547 | PF00917 | 0.325 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.344 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.300 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.354 |
LIG_14-3-3_CanoR_1 | 251 | 259 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 38 | 44 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 465 | 473 | PF00244 | 0.325 |
LIG_14-3-3_CanoR_1 | 50 | 58 | PF00244 | 0.583 |
LIG_Actin_WH2_2 | 371 | 387 | PF00022 | 0.300 |
LIG_AP2alpha_1 | 368 | 372 | PF02296 | 0.300 |
LIG_AP2alpha_1 | 573 | 577 | PF02296 | 0.414 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.547 |
LIG_BIR_III_2 | 180 | 184 | PF00653 | 0.610 |
LIG_BRCT_BRCA1_1 | 466 | 470 | PF00533 | 0.277 |
LIG_BRCT_BRCA1_1 | 505 | 509 | PF00533 | 0.414 |
LIG_deltaCOP1_diTrp_1 | 460 | 470 | PF00928 | 0.282 |
LIG_EH1_1 | 372 | 380 | PF00400 | 0.360 |
LIG_eIF4E_1 | 373 | 379 | PF01652 | 0.282 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.493 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.600 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.582 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.485 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.300 |
LIG_FHA_1 | 558 | 564 | PF00498 | 0.404 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.576 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.643 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.612 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.660 |
LIG_FHA_2 | 634 | 640 | PF00498 | 0.589 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.586 |
LIG_LIR_Apic_2 | 513 | 519 | PF02991 | 0.301 |
LIG_LIR_Apic_2 | 535 | 541 | PF02991 | 0.268 |
LIG_LIR_Gen_1 | 380 | 388 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 467 | 477 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 380 | 384 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 467 | 473 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 513 | 518 | PF02991 | 0.338 |
LIG_OCRL_FandH_1 | 360 | 372 | PF00620 | 0.282 |
LIG_Pex14_2 | 285 | 289 | PF04695 | 0.523 |
LIG_Pex14_2 | 368 | 372 | PF04695 | 0.300 |
LIG_Pex14_2 | 573 | 577 | PF04695 | 0.374 |
LIG_Pex14_2 | 579 | 583 | PF04695 | 0.343 |
LIG_PTAP_UEV_1 | 104 | 109 | PF05743 | 0.509 |
LIG_PTB_Apo_2 | 283 | 290 | PF02174 | 0.585 |
LIG_PTB_Apo_2 | 301 | 308 | PF02174 | 0.417 |
LIG_PTB_Apo_2 | 440 | 447 | PF02174 | 0.414 |
LIG_PTB_Phospho_1 | 301 | 307 | PF10480 | 0.416 |
LIG_SH2_CRK | 307 | 311 | PF00017 | 0.365 |
LIG_SH2_CRK | 529 | 533 | PF00017 | 0.414 |
LIG_SH2_STAP1 | 642 | 646 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.768 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 581 | 584 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 610 | 613 | PF00017 | 0.414 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.623 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.743 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.629 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.504 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.318 |
LIG_SH3_3 | 504 | 510 | PF00018 | 0.381 |
LIG_SUMO_SIM_anti_2 | 115 | 120 | PF11976 | 0.395 |
LIG_SUMO_SIM_anti_2 | 404 | 409 | PF11976 | 0.314 |
LIG_SUMO_SIM_anti_2 | 498 | 506 | PF11976 | 0.365 |
LIG_SUMO_SIM_par_1 | 115 | 120 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 15 | 23 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 618 | 624 | PF11976 | 0.334 |
LIG_TRAF2_1 | 585 | 588 | PF00917 | 0.282 |
LIG_TRAF2_1 | 636 | 639 | PF00917 | 0.633 |
LIG_TRAF2_1 | 9 | 12 | PF00917 | 0.553 |
LIG_UBA3_1 | 334 | 342 | PF00899 | 0.457 |
LIG_UBA3_1 | 411 | 415 | PF00899 | 0.311 |
LIG_WRC_WIRS_1 | 311 | 316 | PF05994 | 0.475 |
LIG_WRC_WIRS_1 | 378 | 383 | PF05994 | 0.282 |
LIG_WRC_WIRS_1 | 512 | 517 | PF05994 | 0.300 |
MOD_CDC14_SPxK_1 | 196 | 199 | PF00782 | 0.619 |
MOD_CDC14_SPxK_1 | 43 | 46 | PF00782 | 0.544 |
MOD_CDK_SPxK_1 | 193 | 199 | PF00069 | 0.624 |
MOD_CDK_SPxK_1 | 384 | 390 | PF00069 | 0.300 |
MOD_CDK_SPxK_1 | 40 | 46 | PF00069 | 0.536 |
MOD_CDK_SPxxK_3 | 520 | 527 | PF00069 | 0.325 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.562 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.651 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.632 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.428 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.395 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.802 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.799 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.732 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.600 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.740 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.568 |
MOD_CK2_1 | 633 | 639 | PF00069 | 0.651 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.738 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.543 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.451 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.714 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.617 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.663 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.776 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.319 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.322 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.452 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.360 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.679 |
MOD_GlcNHglycan | 597 | 600 | PF01048 | 0.392 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.362 |
MOD_GlcNHglycan | 64 | 68 | PF01048 | 0.710 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.724 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.629 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.437 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.423 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.543 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.593 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.728 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.762 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.492 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.355 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.836 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.311 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.665 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.652 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.529 |
MOD_N-GLC_1 | 222 | 227 | PF02516 | 0.753 |
MOD_N-GLC_1 | 39 | 44 | PF02516 | 0.748 |
MOD_N-GLC_1 | 442 | 447 | PF02516 | 0.414 |
MOD_N-GLC_1 | 543 | 548 | PF02516 | 0.414 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.756 |
MOD_N-GLC_2 | 318 | 320 | PF02516 | 0.387 |
MOD_N-GLC_2 | 336 | 338 | PF02516 | 0.456 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.546 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.566 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.690 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.648 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.354 |
MOD_NEK2_1 | 564 | 569 | PF00069 | 0.289 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.362 |
MOD_NEK2_1 | 605 | 610 | PF00069 | 0.331 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.753 |
MOD_NEK2_2 | 410 | 415 | PF00069 | 0.381 |
MOD_NEK2_2 | 442 | 447 | PF00069 | 0.300 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.702 |
MOD_PK_1 | 350 | 356 | PF00069 | 0.403 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.662 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.548 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.694 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.497 |
MOD_PKA_2 | 464 | 470 | PF00069 | 0.325 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.360 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.841 |
MOD_PKA_2 | 557 | 563 | PF00069 | 0.325 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.667 |
MOD_PKB_1 | 50 | 58 | PF00069 | 0.616 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.483 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.540 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.653 |
MOD_Plk_1 | 401 | 407 | PF00069 | 0.282 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.282 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.282 |
MOD_Plk_2-3 | 543 | 549 | PF00069 | 0.331 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.476 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.354 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.296 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.300 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.478 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.655 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.616 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.511 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.435 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.340 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.300 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.745 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.354 |
MOD_SUMO_rev_2 | 339 | 344 | PF00179 | 0.402 |
TRG_DiLeu_BaEn_3 | 339 | 345 | PF01217 | 0.376 |
TRG_DiLeu_BaLyEn_6 | 625 | 630 | PF01217 | 0.344 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.360 |
TRG_ER_diArg_1 | 259 | 261 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 49 | 52 | PF00400 | 0.688 |
TRG_Pf-PMV_PEXEL_1 | 16 | 21 | PF00026 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 267 | 272 | PF00026 | 0.547 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5U5 | Leptomonas seymouri | 73% | 96% |
A0A0S4IYE4 | Bodo saltans | 56% | 100% |
A0A0S4J323 | Bodo saltans | 27% | 100% |
A0A1X0NPA5 | Trypanosomatidae | 57% | 100% |
A0A3Q8I8M6 | Leishmania donovani | 33% | 100% |
A0A3R7NXP6 | Trypanosoma rangeli | 56% | 100% |
A0A3S5H6D4 | Leishmania donovani | 97% | 100% |
A4H5M4 | Leishmania braziliensis | 85% | 100% |
A4HTW1 | Leishmania infantum | 96% | 100% |
A4HVT0 | Leishmania infantum | 33% | 100% |
D0A9C5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9AMP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9APH5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
Q4QG03 | Leishmania major | 33% | 100% |